Spermatogenic Failure, Y-linked, 2; Spgfy2
About 2 to 3% of human males are infertile because of defects in sperm function, primarily due to oligozoospermia (defined as less than 10-15 million sperm per mL of semen) or azoospermia (Hull et al., 1985).
Genes related to Spermatogenic Failure, Y-linked, 2; Spgfy2
Clinical FeaturesPhenotypes and symptoms related to Spermatogenic Failure, Y-linked, 2; Spgfy2
- Male infertility
- Abnormal sperm morphology
Incidence and onset information— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.
Spermatogenic Failure, Y-linked, 2; Spgfy2 Is also known as oligozoospermia, nonobstructive, y-linked, spermatogenic arrest, y-linked, azoospermia, nonobstructive, y-linked, spermatogenic failure, nonobstructive, y-linked, oligospermia, nonobstructive, y-linked.
Researches and researchersCurrently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.
Spermatogenic Failure, Y-linked, 2; Spgfy2 Recommended genes panels
|Panel Name, Specifity and genes Tested/covered|
Spermatogenic Failure , Panel Massive Sequencing (NGS) 9 Genes.
By Reference Laboratory Genetics (Spain).
AURKC, USP9Y, CATSPER1, SYCP3, KLHL10, DPY19L2, SEPT12, SPATA16, NR5A1
Phosphorus Male Infertility Panel.
By Phosphorus Diagnostics LLC (United States).
SRY, AURKC, USP9Y, CATSPER1, CFTR, DPY19L2, FSHB, FSHR, AR, LHCGR
Tempus xO assay.
By Tempus Labs, Inc. (United States).
BCL6, RHEB, RIPK1, RIPK2, RIPK3, RIT1, BCL7A, BCL9, BCR, ROBO2, ROCK1, ROCK2, ROR1, ROR2, ROS1, RPA1, BDNF, RPL5, RPN1, RPS6KB1 , (...)
View the complete list with 1627 more genes
You can get up to -5 more panels with our dedicated toolLearn more
Sources and references
You can check the following sources for additional information.OMIM MESH Rare Disease Symptoms Checker
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like UNCOMBABLE HAIR SYNDROME 3; UHS3 INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY; FBP1D JOUBERT SYNDROME 10; JBTS10 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20; COXPD20 JOUBERT SYNDROME 1; JBTS1